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Clinical Trial Summary

This is a randomized, double-blind, positive controlled design clinical trial of tetanus vaccine, adsorbed manufactured by Sinovac Life Sciences Co., Ltd.The purpose of this study is to evaluate the safety and immunogenicity of tetanus vaccine, adsorbed in 18~44 years old population.


Clinical Trial Description

This is a randomized, double-blind, positive controlled design clinical trial of tetanus vaccine, adsorbed.The purpose of this study is to evaluate the safety and immunogenicity of tetanus vaccine, adsorbed in 18~44 years old population.The study will conduct in two phases.A total of 1260 subjects including 60 subjects in phase Ⅰ and 1200 subjects in phase III will be enrolled.All of subjects in phase Ⅰ and phase III will be randomly assigned 2 groups in a 1:1 ratio to receive one dose of experimental vaccine or control vaccine. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06049940
Study type Interventional
Source Sinovac Biotech Co., Ltd
Contact Zhiqiang Xie
Phone 13526534586
Email xiezqshang@163.com
Status Recruiting
Phase Phase 3
Start date September 1, 2023
Completion date March 30, 2025

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